| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:5260646-5261055 | Common:5; Rare:148; Clinvar (benign):4 | ||||
| chr6:7107532-7107851 | Rare:111 | ||||
| chr6:7108272-7108484 | Rare:63 | ||||
| chr6:7108577-7108681 | Rare:36 | ||||
| chr6:7313042-7313380 | Common:5; Rare:126 | ||||
| chr6:7389748-7389986 | Common:1; Rare:59 | ||||
| chr6:7541391-7541778 | Rare:119; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:7541797-7541938 | Common:2; Rare:44; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:7910625-7910888 | Common:4; Rare:105 | ||||
| chr6:8064326-8064485 | Common:4; Rare:65 | ||||
| chr6:8102433-8102749 | Common:1; Rare:112 | ||||
| chr6:8435413-8435659 | Common:4; Rare:87 | ||||
| chr6:10694586-10694984 | Common:5; Rare:111 | ||||
| chr6:10722817-10723241 | Common:6; Rare:143 | ||||
| chr6:10747571-10747869 | Common:4; Rare:116 |